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Netrin-4 activates endothelial integrin {alpha}6{beta}1.


ABSTRACT: Netrin-4 regulates vascular development. Identity of netrin-4 endothelial receptor and its subsequent cell functions is controversial. We previously demonstrated that the inhibition of netrin-1 canonical receptors, Unc5B and neogenin, expressed by lymphatic endothelial cells, do not suppress netrin-4-induced cell signaling and functions. Netrin family members were shown to signal through a range of receptors, including integrins (such as ?3?1, ?6?1, and ?6?4) in nonendothelial cells.We tested whether integrins are netrin-4 receptors in the endothelium.The ?6?1 integrin is expressed by endothelial cells, and binds netrin-4 in a dose-dependent manner. Inhibition of ?6 or ?1 integrin subunits suppresses netrin-4-induced endothelial cell migration, adhesion, and focal adhesion contact. Netrin-4-stimulated phosphorylation of Src kinase family, effectors of endothelial cell migration, is also abolished by ?6 or ?1 inhibition. Finally, netrin-4 and ?6?1 integrin expression colocalize in mouse embryonic, intestine, and tumor vasculature.The ?6?1 integrin is a netrin-4 receptor in lymphatic endothelium and consequently represents a potential target to inhibit netrin-4-induced metastatic dissemination.

SUBMITTER: Larrieu-Lahargue F 

PROVIDER: S-EPMC3552560 | biostudies-literature | 2011 Sep

REPOSITORIES: biostudies-literature

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Netrin-4 activates endothelial integrin {alpha}6{beta}1.

Larrieu-Lahargue Frederic F   Welm Alana L AL   Thomas Kirk R KR   Li Dean Y DY  

Circulation research 20110728 7


<h4>Rationale</h4>Netrin-4 regulates vascular development. Identity of netrin-4 endothelial receptor and its subsequent cell functions is controversial. We previously demonstrated that the inhibition of netrin-1 canonical receptors, Unc5B and neogenin, expressed by lymphatic endothelial cells, do not suppress netrin-4-induced cell signaling and functions. Netrin family members were shown to signal through a range of receptors, including integrins (such as α3β1, α6β1, and α6β4) in nonendothelial  ...[more]

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